Molecular Investigation of GB Virus C RNA in Hemodialysis and Thalassemics Patients from Brazil

The GB virus C (GBV-C) hepatitis G virus (HGV) is a member of the Flaviviridae family. Based on the clinical and epidemiological profiles, this virus could be acquired mainly by parenteral transmission through contaminated blood. We therefore investigated the presence of GBV-C HGV and its relation w...

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Veröffentlicht in:Renal failure 2003, Vol.25 (1), p.67-75
Hauptverfasser: Watanabe, Maria Angelica Ehara, Milanezi, Cristiane Maria, Araújo Silva, Wilson, de Lucena Ângulo, Ivan, Santis, Gil, Kashima, Simone, Cardeal da Costa, José Abrão, Neto, Miguel Abrão, Covas, Dimas Tadeu
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container_end_page 75
container_issue 1
container_start_page 67
container_title Renal failure
container_volume 25
creator Watanabe, Maria Angelica Ehara
Milanezi, Cristiane Maria
Araújo Silva, Wilson
de Lucena Ângulo, Ivan
Santis, Gil
Kashima, Simone
Cardeal da Costa, José Abrão
Neto, Miguel Abrão
Covas, Dimas Tadeu
description The GB virus C (GBV-C) hepatitis G virus (HGV) is a member of the Flaviviridae family. Based on the clinical and epidemiological profiles, this virus could be acquired mainly by parenteral transmission through contaminated blood. We therefore investigated the presence of GBV-C HGV and its relation with the other blood borne viruses as hepatitis B and C viruses (HBV, HCV) in hemodialysis and thalassemic individuals and blood donors from Ribeirão Preto--Brazil. Detection of blood borne virus markers including HBV surface antigen (HbsAg), HBV core antibody (anti-Hbc) and HCV antibody was carried out. HIV-1, HIV-2, HTLV-1 and HTLV-2 were also investigated. GBV-C HGV RNA was detected by reverse transcriptase and polymerase chain reaction (RT-PCR). Ninety-four serum samples from patients with chronic renal failure were analyzed. GBV-C HGV RNA was identified in 12 (12.8%) patients, anti-HCV antibodies in 28 (29.8%), anti-Hbc in 9 (9.6%), anti-HIV in 1 (1%), HBsAg in 33 (35.1%), and HBsAg anti-HBc was observed in 2 (2.1%) patients. Thirty-six (38.3%) samples were non-reactive. Seven of the 12 GBV-C HGV RNA infected samples were co-infected with other viruses: 3 (25%) with HBsAg, 2 (16.7%) with anti-HCV and 2 (16.7%) with anti-HBc anti-HCV HBsAg. Among the 42 thalassemic patients, GBV-C HGV RNA was detected in 6 42 patients (14.2 %). Three patients presented GBV-C HGV, with other blood borne markers. We also detected GBV-C HGV in 6 50 (12%) blood donors. In these GBV-C HGV positive thalassemics patients, 50% (3 6) were young individuals (lesser 15 years old) and 67% (4 6) were female patients. The presence of GBV-C RNA in the absence of hepatitis B and C infection in the young patients and healthy donors could be indicate that this virus is capable of independent transmission and does not contribute to liver disease.
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Based on the clinical and epidemiological profiles, this virus could be acquired mainly by parenteral transmission through contaminated blood. We therefore investigated the presence of GBV-C HGV and its relation with the other blood borne viruses as hepatitis B and C viruses (HBV, HCV) in hemodialysis and thalassemic individuals and blood donors from Ribeirão Preto--Brazil. Detection of blood borne virus markers including HBV surface antigen (HbsAg), HBV core antibody (anti-Hbc) and HCV antibody was carried out. HIV-1, HIV-2, HTLV-1 and HTLV-2 were also investigated. GBV-C HGV RNA was detected by reverse transcriptase and polymerase chain reaction (RT-PCR). Ninety-four serum samples from patients with chronic renal failure were analyzed. GBV-C HGV RNA was identified in 12 (12.8%) patients, anti-HCV antibodies in 28 (29.8%), anti-Hbc in 9 (9.6%), anti-HIV in 1 (1%), HBsAg in 33 (35.1%), and HBsAg anti-HBc was observed in 2 (2.1%) patients. Thirty-six (38.3%) samples were non-reactive. Seven of the 12 GBV-C HGV RNA infected samples were co-infected with other viruses: 3 (25%) with HBsAg, 2 (16.7%) with anti-HCV and 2 (16.7%) with anti-HBc anti-HCV HBsAg. Among the 42 thalassemic patients, GBV-C HGV RNA was detected in 6 42 patients (14.2 %). Three patients presented GBV-C HGV, with other blood borne markers. We also detected GBV-C HGV in 6 50 (12%) blood donors. In these GBV-C HGV positive thalassemics patients, 50% (3 6) were young individuals (lesser 15 years old) and 67% (4 6) were female patients. 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Based on the clinical and epidemiological profiles, this virus could be acquired mainly by parenteral transmission through contaminated blood. We therefore investigated the presence of GBV-C HGV and its relation with the other blood borne viruses as hepatitis B and C viruses (HBV, HCV) in hemodialysis and thalassemic individuals and blood donors from Ribeirão Preto--Brazil. Detection of blood borne virus markers including HBV surface antigen (HbsAg), HBV core antibody (anti-Hbc) and HCV antibody was carried out. HIV-1, HIV-2, HTLV-1 and HTLV-2 were also investigated. GBV-C HGV RNA was detected by reverse transcriptase and polymerase chain reaction (RT-PCR). Ninety-four serum samples from patients with chronic renal failure were analyzed. GBV-C HGV RNA was identified in 12 (12.8%) patients, anti-HCV antibodies in 28 (29.8%), anti-Hbc in 9 (9.6%), anti-HIV in 1 (1%), HBsAg in 33 (35.1%), and HBsAg anti-HBc was observed in 2 (2.1%) patients. Thirty-six (38.3%) samples were non-reactive. Seven of the 12 GBV-C HGV RNA infected samples were co-infected with other viruses: 3 (25%) with HBsAg, 2 (16.7%) with anti-HCV and 2 (16.7%) with anti-HBc anti-HCV HBsAg. Among the 42 thalassemic patients, GBV-C HGV RNA was detected in 6 42 patients (14.2 %). Three patients presented GBV-C HGV, with other blood borne markers. We also detected GBV-C HGV in 6 50 (12%) blood donors. In these GBV-C HGV positive thalassemics patients, 50% (3 6) were young individuals (lesser 15 years old) and 67% (4 6) were female patients. The presence of GBV-C RNA in the absence of hepatitis B and C infection in the young patients and healthy donors could be indicate that this virus is capable of independent transmission and does not contribute to liver disease.</description><subject>Adult</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Blood donors</subject><subject>Blood-borne diseases</subject><subject>Brazil - epidemiology</subject><subject>Chronic renal failure</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Female</subject><subject>Flaviviridae Infections - blood</subject><subject>Flaviviridae Infections - diagnosis</subject><subject>Flaviviridae Infections - immunology</subject><subject>GB virus C - genetics</subject><subject>GB virus C - immunology</subject><subject>GBV-C/HGV</subject><subject>HBV</subject><subject>HCV</subject><subject>Hepacivirus - genetics</subject><subject>Hepacivirus - immunology</subject><subject>Hepatitis Antibodies - blood</subject><subject>Hepatitis Antibodies - immunology</subject><subject>Hepatitis B - blood</subject><subject>Hepatitis B - diagnosis</subject><subject>Hepatitis B - immunology</subject><subject>Hepatitis B virus - genetics</subject><subject>Hepatitis B virus - immunology</subject><subject>Hepatitis C - blood</subject><subject>Hepatitis C - diagnosis</subject><subject>Hepatitis C - immunology</subject><subject>Hepatitis, Viral, Human - blood</subject><subject>Hepatitis, Viral, Human - diagnosis</subject><subject>Hepatitis, Viral, Human - immunology</subject><subject>HGV</subject><subject>Humans</subject><subject>Intensive care medicine</subject><subject>Kidney Failure, Chronic - blood</subject><subject>Kidney Failure, Chronic - immunology</subject><subject>Kidney Failure, Chronic - therapy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular Diagnostic Techniques</subject><subject>Prevalence</subject><subject>Renal Dialysis</subject><subject>RNA, Viral - blood</subject><subject>RNA, Viral - immunology</subject><subject>Thalassemia</subject><subject>Thalassemia - blood</subject><subject>Thalassemia - immunology</subject><subject>Thalassemia - therapy</subject><subject>Transfusion Reaction</subject><subject>Tropical medicine</subject><issn>0886-022X</issn><issn>1525-6049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kDtvFDEUhS1ERJZASYvcQDfEr5nxlMkCyUbhIRQQnXXXD9aRx07sGdDm12O0CxFFqtt85-ieD6EXlLyhRNLji7erhjJCaC-64RFa0Ja1TUfE8BgtiJRdQxj7foielnJdoVb27Ak6pKyjPedigdSHFKyeA2S8ij9tmfwPmHyKODl8doq_-TwXvMRfPp5gH_G5HZPxELbFFwzR4KsNBCjFjl4X_LkmbZwKdjmN-DTDnQ_P0IGDUOzz_T1CX9-_u1qeN5efzlbLk8tGi7adGmu0dIyTNZEDtKJlzNi6oeWc8M5Stx6ENEJL3TlB2MDXrqdGuKHTZqCDHPgRer3rvcnpdq471OiLtiFAtGkuquekJ1TSCjY7UOdUSrZO3WQ_Qt4qStQfo6oaVf-MVv7lvnhej9bc03uFFXi1B6BoCC5D1L7cc3UMqSMqJ3ecjy7lEX6lHIyaYBtS_hviD_3Q_xfdWAjTRkO26jrNOVaxD3z_GxQKoVA</recordid><startdate>2003</startdate><enddate>2003</enddate><creator>Watanabe, Maria Angelica Ehara</creator><creator>Milanezi, Cristiane Maria</creator><creator>Araújo Silva, Wilson</creator><creator>de Lucena Ângulo, Ivan</creator><creator>Santis, Gil</creator><creator>Kashima, Simone</creator><creator>Cardeal da Costa, José Abrão</creator><creator>Neto, Miguel Abrão</creator><creator>Covas, Dimas Tadeu</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2003</creationdate><title>Molecular Investigation of GB Virus C RNA in Hemodialysis and Thalassemics Patients from Brazil</title><author>Watanabe, Maria Angelica Ehara ; Milanezi, Cristiane Maria ; Araújo Silva, Wilson ; de Lucena Ângulo, Ivan ; Santis, Gil ; Kashima, Simone ; Cardeal da Costa, José Abrão ; Neto, Miguel Abrão ; Covas, Dimas Tadeu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-edc8f230b089a54522de049533036e1fb948d4c8c6f40293bf71d4f96cd919893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adult</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Blood donors</topic><topic>Blood-borne diseases</topic><topic>Brazil - epidemiology</topic><topic>Chronic renal failure</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Female</topic><topic>Flaviviridae Infections - blood</topic><topic>Flaviviridae Infections - diagnosis</topic><topic>Flaviviridae Infections - immunology</topic><topic>GB virus C - genetics</topic><topic>GB virus C - immunology</topic><topic>GBV-C/HGV</topic><topic>HBV</topic><topic>HCV</topic><topic>Hepacivirus - genetics</topic><topic>Hepacivirus - immunology</topic><topic>Hepatitis Antibodies - blood</topic><topic>Hepatitis Antibodies - immunology</topic><topic>Hepatitis B - blood</topic><topic>Hepatitis B - diagnosis</topic><topic>Hepatitis B - immunology</topic><topic>Hepatitis B virus - genetics</topic><topic>Hepatitis B virus - immunology</topic><topic>Hepatitis C - blood</topic><topic>Hepatitis C - diagnosis</topic><topic>Hepatitis C - immunology</topic><topic>Hepatitis, Viral, Human - blood</topic><topic>Hepatitis, Viral, Human - diagnosis</topic><topic>Hepatitis, Viral, Human - immunology</topic><topic>HGV</topic><topic>Humans</topic><topic>Intensive care medicine</topic><topic>Kidney Failure, Chronic - blood</topic><topic>Kidney Failure, Chronic - immunology</topic><topic>Kidney Failure, Chronic - therapy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Molecular Diagnostic Techniques</topic><topic>Prevalence</topic><topic>Renal Dialysis</topic><topic>RNA, Viral - blood</topic><topic>RNA, Viral - immunology</topic><topic>Thalassemia</topic><topic>Thalassemia - blood</topic><topic>Thalassemia - immunology</topic><topic>Thalassemia - therapy</topic><topic>Transfusion Reaction</topic><topic>Tropical medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Watanabe, Maria Angelica Ehara</creatorcontrib><creatorcontrib>Milanezi, Cristiane Maria</creatorcontrib><creatorcontrib>Araújo Silva, Wilson</creatorcontrib><creatorcontrib>de Lucena Ângulo, Ivan</creatorcontrib><creatorcontrib>Santis, Gil</creatorcontrib><creatorcontrib>Kashima, Simone</creatorcontrib><creatorcontrib>Cardeal da Costa, José Abrão</creatorcontrib><creatorcontrib>Neto, Miguel Abrão</creatorcontrib><creatorcontrib>Covas, Dimas Tadeu</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Renal failure</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Watanabe, Maria Angelica Ehara</au><au>Milanezi, Cristiane Maria</au><au>Araújo Silva, Wilson</au><au>de Lucena Ângulo, Ivan</au><au>Santis, Gil</au><au>Kashima, Simone</au><au>Cardeal da Costa, José Abrão</au><au>Neto, Miguel Abrão</au><au>Covas, Dimas Tadeu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Investigation of GB Virus C RNA in Hemodialysis and Thalassemics Patients from Brazil</atitle><jtitle>Renal failure</jtitle><addtitle>Ren Fail</addtitle><date>2003</date><risdate>2003</risdate><volume>25</volume><issue>1</issue><spage>67</spage><epage>75</epage><pages>67-75</pages><issn>0886-022X</issn><eissn>1525-6049</eissn><coden>REFAE8</coden><abstract>The GB virus C (GBV-C) hepatitis G virus (HGV) is a member of the Flaviviridae family. Based on the clinical and epidemiological profiles, this virus could be acquired mainly by parenteral transmission through contaminated blood. We therefore investigated the presence of GBV-C HGV and its relation with the other blood borne viruses as hepatitis B and C viruses (HBV, HCV) in hemodialysis and thalassemic individuals and blood donors from Ribeirão Preto--Brazil. Detection of blood borne virus markers including HBV surface antigen (HbsAg), HBV core antibody (anti-Hbc) and HCV antibody was carried out. HIV-1, HIV-2, HTLV-1 and HTLV-2 were also investigated. GBV-C HGV RNA was detected by reverse transcriptase and polymerase chain reaction (RT-PCR). Ninety-four serum samples from patients with chronic renal failure were analyzed. GBV-C HGV RNA was identified in 12 (12.8%) patients, anti-HCV antibodies in 28 (29.8%), anti-Hbc in 9 (9.6%), anti-HIV in 1 (1%), HBsAg in 33 (35.1%), and HBsAg anti-HBc was observed in 2 (2.1%) patients. Thirty-six (38.3%) samples were non-reactive. Seven of the 12 GBV-C HGV RNA infected samples were co-infected with other viruses: 3 (25%) with HBsAg, 2 (16.7%) with anti-HCV and 2 (16.7%) with anti-HBc anti-HCV HBsAg. Among the 42 thalassemic patients, GBV-C HGV RNA was detected in 6 42 patients (14.2 %). Three patients presented GBV-C HGV, with other blood borne markers. We also detected GBV-C HGV in 6 50 (12%) blood donors. In these GBV-C HGV positive thalassemics patients, 50% (3 6) were young individuals (lesser 15 years old) and 67% (4 6) were female patients. The presence of GBV-C RNA in the absence of hepatitis B and C infection in the young patients and healthy donors could be indicate that this virus is capable of independent transmission and does not contribute to liver disease.</abstract><cop>Colchester</cop><pub>Informa UK Ltd</pub><pmid>12617334</pmid><doi>10.1081/JDI-120017469</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Biomarkers - blood
Blood donors
Blood-borne diseases
Brazil - epidemiology
Chronic renal failure
Emergency and intensive care: renal failure. Dialysis management
Female
Flaviviridae Infections - blood
Flaviviridae Infections - diagnosis
Flaviviridae Infections - immunology
GB virus C - genetics
GB virus C - immunology
GBV-C/HGV
HBV
HCV
Hepacivirus - genetics
Hepacivirus - immunology
Hepatitis Antibodies - blood
Hepatitis Antibodies - immunology
Hepatitis B - blood
Hepatitis B - diagnosis
Hepatitis B - immunology
Hepatitis B virus - genetics
Hepatitis B virus - immunology
Hepatitis C - blood
Hepatitis C - diagnosis
Hepatitis C - immunology
Hepatitis, Viral, Human - blood
Hepatitis, Viral, Human - diagnosis
Hepatitis, Viral, Human - immunology
HGV
Humans
Intensive care medicine
Kidney Failure, Chronic - blood
Kidney Failure, Chronic - immunology
Kidney Failure, Chronic - therapy
Male
Medical sciences
Middle Aged
Molecular Diagnostic Techniques
Prevalence
Renal Dialysis
RNA, Viral - blood
RNA, Viral - immunology
Thalassemia
Thalassemia - blood
Thalassemia - immunology
Thalassemia - therapy
Transfusion Reaction
Tropical medicine
title Molecular Investigation of GB Virus C RNA in Hemodialysis and Thalassemics Patients from Brazil
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